The European Commission's latest report into the workings of pharmaceutical parallel trade has found evidence that it "brings a considerable risk for the safety of the patients," according to the Commission's Vice President, Gunter Verheugen. He added that "the reasons for that are numerous, eg, there are problems with the packaging and labeling of the products as well as with product recalls, the complexity of distribution channels and the supply."
Commissioner Verheugen was responding to a written question from Mairead McGuinness, a Member of the European Parliament representing East Leinster, Ireland, for the Fine Gael, affiliated to the European People's Party. In her original inquiry, Ms McGuinness noted that the rate of wholesaler markups in Ireland is 17.66%, or double the European Union average, which in turn creates a market for parallel trade.
The EC is analyzing the results of the study with the intention of developing a coherent strategy to avoid the risks to the supply chain that are attributable to prescription drug re-importation.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2025 | Headless Content Management with Blaze